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    MicroRNAs in platelet function and cardiovascular disease

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    Authors
    McManus, David D.
    Freedman, Jane
    UMass Chan Affiliations
    Department of Medicine, Division of Cardiovascular Medicine
    Document Type
    Journal Article
    Publication Date
    2015-12-01
    Keywords
    UMCCTS funding
    Cardiology
    Cardiovascular Diseases
    Medical Genetics
    
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    Link to Full Text
    http://dx.doi.org/10.1038/nrcardio.2015.101
    Abstract
    Cardiovascular disease-a leading cause of morbidity and mortality among adults-is strongly influenced by platelet function through acute thrombotic and atherogenic mechanisms. Pathways that regulate platelet activity and lead to coronary occlusion are central to the pathogenesis of acute coronary syndromes. Platelet activation contributes to other thrombotic disorders and cardiovascular diseases, including stroke. Anucleate platelets are now understood to contain transcripts that might relate to other physiological or pathophysiological conditions, be released into the circulation, participate in protein formation, and engage in horizontal RNA transfer to other vascular cells. These platelet transcripts include microRNAs (miRNAs), which are small noncoding RNAs involved in many molecular processes, most notably regulation of gene expression. In platelets, these noncoding RNAs seem to participate in vascular homeostasis, inflammation, and platelet function. In addition, levels of platelet miRNAs in the circulation are associated with the presence or extent of cardiovascular diseases, such as atrial fibrillation and peripheral vascular disease. Accumulating data suggest mechanistic roles for platelet-derived miRNAs in haemostasis, thrombosis, and unstable coronary syndromes. In addition, evidence suggests that platelet-derived miRNAs might have important roles as biomarkers of cardiovascular disease susceptibility, prognosis, or treatment.
    Source
    Nat Rev Cardiol. 2015 Dec;12(12):711-7. doi: 10.1038/nrcardio.2015.101. Epub 2015 Jul 7. Link to article on publisher's site
    DOI
    10.1038/nrcardio.2015.101
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/30567
    PubMed ID
    26149483
    Related Resources
    Link to Article in PubMed
    ae974a485f413a2113503eed53cd6c53
    10.1038/nrcardio.2015.101
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